Frederick Alt, Ph.D.
Charles A. Janeway Professor of Pediatrics, Boston Children's Hospital
Professor of Genetics, Boston Children's Hospital
Charles A. Janeway Professor of Pediatrics and Genetics, Harvard Medical School
The Alt laboratory studies mechanisms that maintain genomic stability in mammalian cells. The programmed recombination and hypermutation events in lymphocytes and the general DNA repair mechanisms involved in these processes are a focus. The laboratory also studies mechanisms that promote and prevent oncogenic translocations. Approaches range from molecular genetics and biochemistry to animal models.
The role of Bruton's tyrosine kinase in B-cell development and function in mice and man.
Authors: Authors: Khan WN, Sideras P, Rosen FS, Alt FW.
Ann N Y Acad Sci
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Ann N Y Acad Sci
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Defective B cell development and function in Btk-deficient mice.
Authors: Authors: Khan WN, Alt FW, Gerstein RM, Malynn BA, Larsson I, Rathbun G, Davidson L, Müller S, Kantor AB, Herzenberg LA, et al.
Immunity
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Immunity
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Potential targets for autosomal SCID mutations.
CD1-restricted T cell recognition of microbial lipoglycan antigens.
Authors: Authors: Sieling PA, Chatterjee D, Porcelli SA, Prigozy TI, Mazzaccaro RJ, Soriano T, Bloom BR, Brenner MB, Kronenberg M, Brennan PJ, et al.
Science
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Science
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Expansions of V alpha 12 CD8+ T-cells in rheumatoid arthritis.
T-cell receptor V beta gene usage in rheumatoid synovial follicles.
Authors: Authors: Travaglio-Encinozal A, Dersimonian H, Jorgensen C, Romagné F, Sany J, D'Angeac AD, Brenner MB, Rème T.
Ann N Y Acad Sci
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Ann N Y Acad Sci
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MHC class I-like, class II-like and CD1 molecules: distinct roles in immunity.
Bclx regulates the survival of double-positive thymocytes.
Authors: Authors: Ma A, Pena JC, Chang B, Margosian E, Davidson L, Alt FW, Thompson CB.
Proc Natl Acad Sci U S A
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Proc Natl Acad Sci U S A
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Natural and synthetic non-peptide antigens recognized by human gamma delta T cells.
Authors: Authors: Tanaka Y, Morita CT, Tanaka Y, Nieves E, Brenner MB, Bloom BR.
Nature
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Nature
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CD3 epsilon and CD3 zeta cytoplasmic domains can independently generate signals for T cell development and function.